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rs111033389

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033389(A;A)
Make rs111033389(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77162989
GeneMYO7A
is asnp
is mentioned by
dbSNPrs111033389
ebirs111033389
HLIrs111033389
Exacrs111033389
Varsomers111033389
Maprs111033389
PheGenIrs111033389
hapmaprs111033389
1000 genomesrs111033389
hgdprs111033389
ensemblrs111033389
gopubmedrs111033389
geneviewrs111033389
scholarrs111033389
googlers111033389
pharmgkbrs111033389
gwascentralrs111033389
openSNPrs111033389
23andMers111033389
23andMe allrs111033389
SNP Nexus

SNPshotrs111033389
SNPdbers111033389
MSV3drs111033389
GWAS Ctlgrs111033389
Max Magnitude0
ClinVar
Risk rs111033389(A;A)
Alt rs111033389(A;A)
Reference rs111033389(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76874035G>A
CLNSRC ClinVar
CLNACC RCV000036059.2,